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The Journal of Clinical Endocrinology and Metabolism
|
October 1, 1996
Analysis of the thyrotropin receptor as a candidate gene in familial Graves' disease
N de Roux, D C Shields, M Misrahi, et al.
Journal of Cardiovascular Pharmacology
|
January 1, 1990
Pathophysiological role of the vascular smooth muscle cell
J B Michel, N De Roux, D Plissonnier, et al.
The New England Journal of Medicine
|
November 27, 1997
A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
N de Roux, J Young, M Misrahi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1996
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism
N de Roux, M Polak, J Couet, et al.
Journal of Medical Genetics
|
June 3, 2004
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
F Kammoun, N de Roux, O Boespflug-Tanguy, et al.
Gut
|
July 17, 2003
Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosis
V Boige, L Castéra, N de Roux, et al.
Hormone Research
|
January 1, 1997
Gonadotrophin and thyrotrophin receptors
E Milgrom, N de Roux, N Ghinea, et al.
European Journal of Endocrinology
|
September 2, 1998
Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomas
P Chanson, N De Roux, J Young, et al.
Annales D'Endocrinologie
|
August 24, 1999
Gonadotropin receptors
M V Hai, N De Roux, N Ghinea, et al.
Neurology
|
April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome
J Nectoux, N Bahi-Buisson, I Guellec, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
The Journal of Clinical Endocrinology and Metabolism
|
October 1, 1996
Analysis of the thyrotropin receptor as a candidate gene in familial Graves' disease
N de Roux, D C Shields, M Misrahi, et al.
Journal of Cardiovascular Pharmacology
|
January 1, 1990
Pathophysiological role of the vascular smooth muscle cell
J B Michel, N De Roux, D Plissonnier, et al.
The New England Journal of Medicine
|
November 27, 1997
A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
N de Roux, J Young, M Misrahi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1996
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism
N de Roux, M Polak, J Couet, et al.
Journal of Medical Genetics
|
June 3, 2004
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
F Kammoun, N de Roux, O Boespflug-Tanguy, et al.
Gut
|
July 17, 2003
Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosis
V Boige, L Castéra, N de Roux, et al.
Hormone Research
|
January 1, 1997
Gonadotrophin and thyrotrophin receptors
E Milgrom, N de Roux, N Ghinea, et al.
European Journal of Endocrinology
|
September 2, 1998
Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomas
P Chanson, N De Roux, J Young, et al.
Annales D'Endocrinologie
|
August 24, 1999
Gonadotropin receptors
M V Hai, N De Roux, N Ghinea, et al.
Neurology
|
April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome
J Nectoux, N Bahi-Buisson, I Guellec, et al.
Page
of 3